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Spots Global Cancer Trial Database for LEGEND Study: EG-70 in NMIBC Patients BCG-Unresponsive and High-Risk NMIBC Incompletely Treated With BCG or BCG-Naïve

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Trial Identification

Brief Title: LEGEND Study: EG-70 in NMIBC Patients BCG-Unresponsive and High-Risk NMIBC Incompletely Treated With BCG or BCG-Naïve

Official Title: A Phase 1/2 Study of EG-70 as an Intravesical Administration to Patients With BCG Unresponsive Non-Muscle Invasive Bladder Cancer (NMIBC) and High-Risk NMIBC Patients Who Are BCG Naïve or Received Incomplete BCG Treatment

Study ID: NCT04752722

Study Description

Brief Summary: This study will evaluate the safety and efficacy of intravesical administration of EG-70 in the bladder and its effect on bladder tumors in patients with NMIBC. This study study consists of two phases; a Phase 1 dose-escalation to establish safety and recommended the phase 2 dose, followed by a Phase 2 study to establish how effective the treatment is. The Study will include patients with NMIBC with Cis for whom BCG therapy is unresponsive and patients with NMIBC with Cis who are BCG-naïve or inadequately treated.

Detailed Description: EG-70 is a novel non-viral gene therapy. EG-70 is designed to elicit a local immune response following delivery of the study gene therapy to the bladder urothelium. This approach of local administration through bladder instillation has the potential to induce a potent immune response exclusively at the site of the tumor, resulting in greater therapeutic benefit while reducing undesirable systemic toxicity. Eligible BCG-unresponsive NMIBC patients will be enrolled in Phase 1, and Cohort 1 of Phase 2. Eligible high-risk NMIBC patients who have been incompletely treated or are BCG-naïve will be enrolled starting in Phase 2 in a separate single-arm cohort (Cohort 2). Patients will be treated for up to four 12-week cycles of study drug instillation doses and assessments with follow up assessments.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Urological Associates of South Arizona, Tucson, Arizona, United States

University of California - Irvine Medical Center, Irvine, California, United States

Urology Group of Southern California / American Institute of Research, Los Angeles, California, United States

USC/Norris Comprehensive Cancer Center, Los Angeles, California, United States

Tower Urology, Los Angeles, California, United States

Genesis Research, San Diego, California, United States

The George Washington Medical Faculty Associates, Washington, District of Columbia, United States

University of Florida, Jacksonville, Florida, United States

Emory University, Atlanta, Georgia, United States

University of Kansas Medical Center, Kansas City, Kansas, United States

Chesapeake Urology Research Associates, Hanover, Maryland, United States

Henry Ford Health System, Detroit, Michigan, United States

Corewell Health Medical Group and Spectrum Health Hospitals, Grand Rapids, Michigan, United States

University of Minnesota, Minneapolis, Minnesota, United States

New Jersey Urology, LLC, Voorhees, New Jersey, United States

Mount Sinai Medical Center, New Haven, New York, United States

Laura & Isaac Perlmutter Cancer Center at NYU Langone Health, New York, New York, United States

UNC Chapel Hill Hospital, Chapel Hill, North Carolina, United States

Associated Urologists of North Carolina, Raleigh, North Carolina, United States

University of Cincinnati Medical Center, Cincinnati, Ohio, United States

Clinical Research Solutions - Helios Clinical Research, Middleburg Heights, Ohio, United States

Oregon Health & Science University (OHSU), Portland, Oregon, United States

Carolina Urologic Research Center, LLC, Myrtle Beach, South Carolina, United States

UT Southwestern Medical Center, Dallas, Texas, United States

Houston Methodist Hospital - Department of Urology, Houston, Texas, United States

University of Texas - MD Anderson Cancer Center, Houston, Texas, United States

Froedtert Hospital / Medical College of Wisconsin, Milwaukee, Wisconsin, United States

Contact Details

Name: Christine Tosone, Ms, RAC

Affiliation: enGene, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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